Cardiac Output Measurement

DEFINITIONS

Q = SV x HR (L/min)

CI = SV x HR/BSA (L/min/m2)

Normal CI = 2.5-4.2

SV = end-diastolic volume – end systolic volume

EF = (SV/EDV) x 100%

Shock = failure of tissue perfusion -> end organ injury

THE FICK PRINCIPLE

  • Adolf Eugen Fick (1829-1901) in 1870, was the first to measure cardiac output
  • assumes oxygen consumption is a function of rate of blood flow and rate of oxygen pick pick up by RBC’s.
  • involves measurement of oxygen concentration of arterial and venous blood and subsequent calculation of O2 consumption.
  • Q can then be derived

Measurements

  • VO2 = oxygen consumption/min (from spirometer with subject rebreathing air through a CO2 absorber)
  • Cv = oxygen content of blood taken from pulmonary artery (deoxygenated)
  • Ca = oxygen content of blood taken from a peripheral artery (oxygenated)

Calculations

VO2 = (Q x Ca) – (Q x Cv)

Therefore,

Q = VO2/(Ca-Cv)

Issues:

  • impractical
  • assumes no shunt (pulmonary blood flow = systemic blood flow)
  • assumes arterial blood is equal to pulmonary venous blood

DILUTION TECHNIQUES

  • known quantity of tracer substance introduced into a space to be measured
  • concentration measured after complete mixing

C1 x V1 = C2 x (V1 + V2)

C1 = initial concentration of indicator
C2 = final concentration of indicator
V1 = volume of indicator
V2 = volume to be measured

  • marker injected proximally to right ventricle and concentration measure distally (pulmonary artery or a peripheral artery)
  • concentration vs time plotted -> integration allow calculation of area under curve (SV x HR = Q)
  • suitable substances: radioiosotope, dye, cold water, temperature of blood.

TECHNIQUES

Clinically Used

  • Non-invasive BP monitoring
  • Central venous monitoring
  • Arterial monitoring
  • Pulmonary arterial monitoring
  • ECHO: TOE and TTE
  • Pulse contour analysis (PiCCO)
  • Oesophageal Doppler
  • Cardiac catheterisation and angiography

Experimental

  • Aortovelography – dopper U/S probe in suprasternal notch to measure blood velocity and acceleration in ascending aorta.
  • Ballistocardiography – detection of body motion due to movement of blood within body with each heart beat.
  • Electromagnetic flow meters
  • Oxygen consumption estimation (Fick)
  • Impedance plethymography

TIPS WHEN USING CARDIAC OUTPUT MONITORS

  • there is no ‘normal’ CVP or wedge -> follow trend and look at the response to treatment
  • abnormal hearts (ischaemic, fibrotic, contused) are less compliant so require higher filling pressures to reach ‘normal’ SV.
  • use SV rather than Q as a response to treatment as Q is calculated from HR which may be fast and mask a poorly performing ventricle.
  • low SvO2 usually indicates under-resuscitation.
  • the first treatment for all shock (including cardiogenic) = volume, volume and more volume.
  • a little extravascular lung water is less harmful than vasoactive drugs.
  • there is no formula to calculate the effect of PEEP on PCWP and CVP -> if kept constant, trend should be consistent.
  • during resuscitation if becomes apparent what CVP the patient ‘likes’ -> aim for this.
  • be cautious of all derived variables, particularly SVR.

Introduction to ICU Series

CCC 700 6

Critical Care

Compendium

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